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Genes upregulated by hypoxia are strategic targets for cancer therapy.

Women's Health Weekly

| January 01, 2004 | COPYRIGHT 2004 NewsRX. This material is published under license from the publisher through the Gale Group, Farmington Hills, Michigan.  All inquiries regarding rights should be directed to the Gale Group. (Hide copyright information)Copyright

2004 JAN 1 - (NewsRx.com & NewsRx.net) -- Genes upregulated by hypoxia are strategic targets for cancer therapy.

According to recent research published in the journal Biomedicine & Pharmacotherapy, "hypoxia is a stress that causes alterations in signal transduction and gene instability. In the cancer microenvironment, hypoxia plays a significant role in forming a tumor phenotype and tumor progression. We aimed to identify the genes upregulated by hypoxia in human breast cancer cell lines, a hormone-dependent MCF-7 and a hormone-independent MDA-MB-231, using microarray analysis."

"These cells were exposed to two oxygen concentrations such as 21% and 1% in a time-course. Out of 12,625 genes, 26 genes were identified as commonly upregulated in both MCF-7 and MDA-MB-231 cells. Some of these genes were already reported as hypoxia-related, but some of those were identified newly," reported H. Bando and colleagues, Tokyo Metropolitan Cancer & Infectious Diseases Center, Breast Cancer Research Group.

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Source: HighBeam Research, Genes upregulated by hypoxia are strategic targets for cancer therapy.

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